Variant report

Variant	nsv1036148
Chromosome Location	chr15:43929339-44014139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
2	ATF2	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43937873-43938217	GM12878	blood:	n/a	n/a
4	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
5	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
6	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
7	BATF	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
9	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
15	BCL3	chr15:44013070-44013288	GM12878	blood:	n/a	n/a
16	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
17	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
18	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
19	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
20	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
21	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
23	CEBPB	chr15:44013072-44013307	A549	lung:	n/a	chr15:44013128-44013139
24	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
25	CEBPB	chr15:44013009-44013290	K562	blood:	n/a	chr15:44013128-44013139
26	CEBPB	chr15:44013108-44013199	IMR90	lung:	n/a	chr15:44013128-44013139
27	CEBPB	chr15:44013006-44013314	HepG2	liver:	n/a	chr15:44013128-44013139
28	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
29	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
30	CTCF	chr15:43941284-43941422	GM19239	blood:	n/a	n/a
31	CTCF	chr15:44010454-44010457	MCF-7	breast:	n/a	n/a
32	CTCF	chr15:43982190-43982491	H1-hESC	embryonic stem cell:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
33	CTCF	chr15:43982246-43982499	A549	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372
34	CTCF	chr15:43982226-43982490	GM10248	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
35	CTCF	chr15:43969453-43969569	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr15:43955748-43955784	MCF-7	breast:	n/a	n/a
37	CTCF	chr15:43941294-43941380	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr15:43969460-43969486	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr15:43994920-43995070	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr15:43941291-43941401	GM12892	blood:	n/a	n/a
41	CTCF	chr15:44003011-44003231	K562	blood:	n/a	n/a
42	CTCF	chr15:43982016-43982654	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
43	CTCF	chr15:43982059-43982069	GM19239	blood:	n/a	n/a
44	CTCF	chr15:43941277-43941388	GM19238	blood:	n/a	n/a
45	CTCF	chr15:43981916-43981941	GM12892	blood:	n/a	n/a
46	CTCF	chr15:44002820-44003337	K562	blood:	n/a	n/a
47	CTCF	chr15:43982161-43982505	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
48	CTCF	chr15:43982204-43982510	Pancreas_OC	pancreas:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
49	CTCF	chr15:43941270-43941358	GM12878	blood:	n/a	n/a
50	CTCF	chr15:44002084-44002092	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43984922-43984972	NHBE	bronchial:	n/a
2	chr15:43941042-43941092	HRE	kidney:	n/a
3	chr15:43941072-43941122	HRE	kidney:	n/a
4	chr15:43941563-43941613	Hepatocyte	liver:	n/a
5	chr15:43937339-43937389	AG09319	gingival:	n/a
6	chr15:43942014-43942064	NH-A	brain:	n/a
7	chr15:43989074-43989124	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:43941642-43941692	HMEC	breast:	n/a
9	chr15:43983306-43983356	A549	lung:	n/a
10	chr15:43984922-43984972	SK-N-MC	brain:	n/a
11	chr15:43940867-43940917	Hepatocyte	liver:	n/a
12	chr15:43937339-43937389	GM06990	blood:	n/a
13	chr15:43991375-43991425	Jurkat	blood:	n/a
14	chr15:43991375-43991425	AG04450	lung:	fetal
15	chr15:43984922-43984972	HCM	heart:	n/a
16	chr15:43941407-43941457	HCF	heart:	n/a
17	chr15:43942014-43942064	HIPEpiC	eye:	n/a
18	chr15:43941072-43941122	HepG2	liver:	n/a
19	chr15:43941072-43941122	HIPEpiC	eye:	n/a
20	chr15:43989074-43989124	HMEC	breast:	n/a
21	chr15:43941034-43941084	GM19239	blood:	n/a
22	chr15:43941042-43941092	Hela-S3	cervix:	n/a
23	chr15:43941034-43941084	NHDF-neo	bronchial:	n/a
24	chr15:43984922-43984972	AoSMC	blood vessel:	n/a
25	chr15:43991375-43991425	K562	blood:	n/a
26	chr15:43942440-43942490	U87	brain:	n/a
27	chr15:43941042-43941092	ECC-1	luminal epithelium:	n/a
28	chr15:43941072-43941122	AG04450	lung:	fetal
29	chr15:43991375-43991425	HAEpiC	amniotic membrane:	n/a
30	chr15:43942014-43942064	GM12891	blood:	n/a
31	chr15:43940867-43940917	NB4	blood:	n/a
32	chr15:43989074-43989124	AG04450	lung:	fetal
33	chr15:43942440-43942490	AG04450	lung:	fetal
34	chr15:43989074-43989124	HCM	heart:	n/a
35	chr15:43941642-43941692	PFSK-1	brain:	n/a
36	chr15:43983306-43983356	Caco-2	colon:	n/a
37	chr15:43991375-43991425	HNPCEpiC	eye:	n/a
38	chr15:43941042-43941092	AG09309	skin:	n/a
39	chr15:43940867-43940917	GM12891	blood:	n/a
40	chr15:43940867-43940917	SKMC	muscle:	n/a
41	chr15:43940140-43940190	GM12891	blood:	n/a
42	chr15:43941871-43941921	BE2_C	brain:	n/a
43	chr15:43931742-43931792	PANC-1	pancreas:	n/a
44	chr15:43941034-43941084	GM12892	blood:	n/a
45	chr15:43940867-43940917	CMK	blood:	n/a
46	chr15:43989074-43989124	NH-A	brain:	n/a
47	chr15:43984922-43984972	PrEC	prostate:	n/a
48	chr15:43937339-43937389	HRPEpiC	eye:	n/a
49	chr15:43941034-43941084	NHBE	bronchial:	n/a
50	chr15:43942014-43942064	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	15:44001645-44015047..15:44080886-44089111	Hela-S3	cervix:
2	chr15:43821060..43823469-chr15:43995355..43996867,2	K562	blood:
3	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
4	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
5	15:43782117-43785993..15:44001645-44015047	GM12878	blood:
6	15:43792489-43802874..15:44001645-44015047	GM12878	blood:
7	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
8	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
9	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
10	15:43807815-43812531..15:44001645-44015047	Hela-S3	cervix:
11	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
12	15:43802874-43806906..15:44001645-44015047	Hela-S3	cervix:

Variant related genes	Relation type
CATSPER2	TF binding region
ENSG00000238494	TF binding region
PDIA3P2	TF binding region
STRC	TF binding region
RNU6-610P	TF binding region
CKMT1A	TF binding region
ENSG00000249839	TF binding region
RNU6-353P	TF binding region
STRCP1	TF binding region
CATSPER2	CpG island
ENSG00000238494	CpG island
PDIA3P2	CpG island
STRC	CpG island
RNU6-610P	CpG island
CKMT1A	CpG island
ENSG00000249839	CpG island
RNU6-353P	CpG island
STRCP1	CpG island
ENSG00000222398	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000237289	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000242866	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000166963	chromatin interactions
ENSG00000206991	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000166762	chromatin interactions

Extended variants
information (count: 1777 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545464969	chr15:43929343-43929344	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs17795279	chr15:43929378-43929379	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs146130677	chr15:43929380-43929381	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs571174037	chr15:43929436-43929437	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs570597493	chr15:43929475-43929476	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs541462702	chr15:43929580-43929581	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs562011661	chr15:43929583-43929584	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs180724504	chr15:43929620-43929621	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs185165817	chr15:43929635-43929636	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs547599189	chr15:43929636-43929637	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs17727979	chr15:43929666-43929667	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs189286348	chr15:43929730-43929731	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs2447193	chr15:43929733-43929734	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs11635852	chr15:43929764-43929765	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs538237616	chr15:43929869-43929870	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs28733321	chr15:43929883-43929884	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs535748097	chr15:43929903-43929904	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370906678	chr15:43929972-43929973	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs568724336	chr15:43929975-43929976	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs556929143	chr15:43929977-43929978	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs182323382	chr15:43929997-43929998	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs576990457	chr15:43930008-43930009	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs372764225	chr15:43930045-43930046	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs545998233	chr15:43930088-43930089	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs35690681	chr15:43930100-43930101	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs555795160	chr15:43930141-43930142	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs576101934	chr15:43930147-43930148	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs541798637	chr15:43930172-43930173	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs149820998	chr15:43930194-43930195	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs527561782	chr15:43930197-43930198	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs541301767	chr15:43930248-43930249	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs550127937	chr15:43930303-43930304	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564385945	chr15:43930333-43930334	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs373950148	chr15:43930339-43930340	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs533118390	chr15:43930341-43930342	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs550002170	chr15:43930342-43930343	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs28642676	chr15:43930372-43930373	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs562991358	chr15:43930417-43930418	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs531748793	chr15:43930425-43930426	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs144510942	chr15:43930466-43930467	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs58177751	chr15:43930487-43930488	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs28418639	chr15:43930488-43930489	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs376047289	chr15:43930489-43930490	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs202120374	chr15:43930498-43930499	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs569983925	chr15:43930555-43930556	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs568338241	chr15:43930569-43930570	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs35028925	chr15:43930606-43930607	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
48	rs142530881	chr15:43930627-43930628	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs570813741	chr15:43930632-43930633	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs539640932	chr15:43930643-43930644	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43914600-43937400	Weak transcription	Fetal Intestine Small	intestine
2	chr15:43915400-43941000	Weak transcription	Hela-S3	cervix
3	chr15:43919600-43941600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:43920400-43941400	Weak transcription	Brain Hippocampus Middle	brain
5	chr15:43921000-43940600	Weak transcription	Gastric	stomach
6	chr15:43921400-43950400	Weak transcription	Aorta	Aorta
7	chr15:43921800-43952600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:43922800-43937600	Weak transcription	Fetal Intestine Large	intestine
9	chr15:43923200-43937400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr15:43923200-43951800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr15:43925200-43939200	Weak transcription	Brain Angular Gyrus	brain
12	chr15:43925200-43939800	Weak transcription	Brain Anterior Caudate	brain
13	chr15:43929600-43940200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr15:43929800-43937600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr15:43930200-43930800	Enhancers	GM12878-XiMat	blood
16	chr15:43930600-43931200	Enhancers	Left Ventricle	heart
17	chr15:43930800-43931400	Flanking Active TSS	GM12878-XiMat	blood
18	chr15:43931000-43931200	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr15:43931000-43931400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:43931000-43931400	Enhancers	Duodenum Mucosa	Duodenum
21	chr15:43931200-43931400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr15:43931200-43943600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr15:43931200-43952000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr15:43931200-43952600	Weak transcription	Left Ventricle	heart
25	chr15:43931400-43939000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr15:43931400-43942400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr15:43932800-43943600	Weak transcription	NHEK	skin
28	chr15:43933800-43941000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr15:43934200-43939200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr15:43934200-43939600	Weak transcription	Lung	lung
31	chr15:43934200-43940200	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr15:43934200-43941400	Weak transcription	Fetal Stomach	stomach
33	chr15:43934200-43941600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr15:43935200-43942200	Weak transcription	Esophagus	oesophagus
35	chr15:43935400-43943200	Weak transcription	Ovary	ovary
36	chr15:43935800-43937400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr15:43935800-43938200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr15:43935800-43940800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr15:43935800-43941000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr15:43935800-43941200	Weak transcription	Fetal Brain Female	brain
41	chr15:43936000-43939600	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr15:43936000-43940200	Weak transcription	Colon Smooth Muscle	Colon
43	chr15:43936000-43940200	Weak transcription	Right Ventricle	heart
44	chr15:43936000-43951800	Weak transcription	Primary T cells from cord blood	blood
45	chr15:43936000-43956000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr15:43936200-43939200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:43936400-43940200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:43936400-43940600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr15:43936400-43943800	Weak transcription	Fetal Brain Male	brain
50	chr15:43937200-43941000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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